Polyp removal device and method of use

ABSTRACT

A device and system for removing polyps is provided and includes a tubular member having proximal and distal ends, a snare portion operably extending from within the distal end of the tubular member, the snare portion including a cutting member for severing the sealed tissue. The polyp removal device may further include a handle portion operatively extending from within the proximal end of the tubular member. The handle portion may be configured for operable engagement by a user and the cutting member may extend between distal ends of the first and second electrodes.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. patent application Ser. No. 13/711,201, filed Dec. 11, 2012, which is a continuation of U.S. patent application Ser. No. 12/363,086, filed Jan. 30, 2009, now U.S. Pat. No. 8,328,809, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/063,158, titled “Endoscopic Flexible Loop for Gastrointestinal Polypectomy and Mucosal Resection Using LigaSure™ Sealing Technology”, by Wexner et al., filed Jan. 31, 2008, the entire contents of these applications are incorporated by reference herein.

TECHNICAL FIELD

The present disclosure relates to devices and methods for the removal of internal tissue and, more particularly, to snare-type devices including a pair of electrodes for treating tissue prior to excision.

BACKGROUND

A polyp is an abnormal growth of tissue projecting from a mucous membrane. A polyp that is attached to the surface of the mucous membrane by a narrow elongated stalk is said to be pedunculated. If no stalk is present, the polyp is said to be sessile. Polyps are commonly found in the colon, stomach, nose, urinary bladder and uterus. Polyps may also form elsewhere in the body where mucous membranes exist, for example, the cervix and small intestine.

The surgical procedure for removing a polyp is generally referred to as a “polypectomy”. Polypectomys are generally endoscopic or laparoscopic procedures performed through the oral or anal cavities. When the location of the polyp permits, the polypectomy may be performed as an open procedure. Conventional polypectomys are completed using various apparatus and techniques known in the art.

As noted above, there are two forms of polyps, sessile and pedunculated. The stalkless or sessile polyps are generally removed using electrical forceps. For example, the excess tissue projecting from the mucous membrane is cauterized and torn from the tissue wall. Pedunculated polyps, or those with stalks, tend to be larger with a greater blood supply. The size and shape of pedunculated polyps typically do not lend themselves to being removed using traditional forceps. Unlike sessile polyps, polyps with a stalk cannot simply be grasped in the jaw members of an electrosurgical forceps and be torn from the tissue wall. Instead, the polypectomy is performed using a surgical snare device.

Conventional snare devices are configured with a snare for looping over the distal end of a hanging polyp and tightening securely around the stalk of the polyp. By constricting the snare, and selectively applying energy to the snare, the device may cauterize or seal the polyp at the stalk as the polyp is severed from the tissue wall. Conventional snare devices may be configured for monopolar or bipolar use. Excising a polyp using a conventional snare device typically involves cutting or otherwise separating the polyp from the tissue wall as the snare device is activated and constricted about the stalk of the polyp. In this manner, the polyp is cauterized as the snare passes through the tissue.

SUMMARY

Disclosed is a device configured for removing polyps. In one embodiment, the polyp removal device includes a tubular member having proximal and distal ends, a snare portion operably extending from within the distal end of the tubular member and including first and second electrodes configured to seal tissue therebetween, the snare portion further including a cutting member for severing the sealed tissue. The polyp removal device may further include a handle portion operatively extending from within the proximal end of the tubular member. The handle portion may be configured for operable engagement by a user. The cutting member may extend between distal ends of the first and second electrodes.

The polyp removal device may be configured to grasp the stalk of a polyp between the first and second electrodes. The first and second electrodes may be hingedly attached to the cutting member. The snare portion may be configured to be retracted within the tubular member. The snare portion may be retracted within the tubular member upon retraction of the handle portion relative to the base portion.

A system including the polyp removal device may further include an electrosurgical generator. The electrodes may be electrically connected to the electrosurgical generator. The distal end of the tubular member may include a spacer member for preventing the first and second electrodes from contacting one another. Alternatively, at least one of the first and second electrodes may include a spacer mounted thereon for preventing contact between the first and second electrodes.

Also provided is a polyp removal device including a tubular member having proximal and distal ends, a handle portion operatively extending from the proximal end of the tubular member, and a snare portion slidably supported within the lumen of the tubular member and operably extending from the distal end of the tubular member, the snare portion including first and second electrodes operably mounted thereto for sealing tissue therebetween, wherein at least one of the first and second electrodes includes at least one spacer mounted thereon for preventing contact between the first and second electrodes. The snare portion of the polyp removal device may be retractable with the tubular member.

Additionally provided is a method of removing a polyp. The method includes the steps of providing a polyp removal device including, a tubular member having proximal and distal ends, a snare portion slidably supported within the lumen of the tubular member and operably extending from the distal end of the tubular member, the snare portion including first and second electrodes operably mounted thereto for sealing tissue therebetween, wherein at least one of the first and second electrodes includes at least one spacer mounted thereon for preventing contact between the first and second electrodes, extending the snare portion relative to the tubular member, looping the snare portion about a portion of a polyp, retracting the snare portion relative to the tubular member to capture the portion of the polyp between the first and second electrodes, and activating the first and second electrodes.

The method may further include the steps of partially advancing the snare portion relative to the tubular member, retracting the tubular member and the snare portion relative to the polyp and severing the polyp from surrounding tissue.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the present disclosure and, together with the detailed description of the embodiments given below, serve to explain the principles of the disclosure.

FIG. 1 is a partial cross-sectional, top plan view of a polyp removal device according to an embodiment of the present disclosure, shown in a first or extended position;

FIG. 2 is a partial cross-sectional top plan view of the polyp removal device of FIG. 1, shown in a partially retracted position;

FIG. 3 is a partial cross-sectional top plan view of the polyp removal device of FIG. 1, shown in a retracted position;

FIG. 4 is a cross-section end view of the polyp removal device of FIGS. 1-3 taken along line 4-4 of FIG. 3;

FIG. 5 is a partial cross-section top plan view of an alternative embodiment of a polyp removal device according to the present disclosure in a completely retracted position;

FIG. 6 is a partial top plan view of the distal end of the polyp removal device of FIGS. 1-4, in a first or extending position about a polyp;

FIG. 7 is a partial top plan view of the distal end of the polyp removal device of FIG. 6, in a retracted position about a polyp;

FIG. 8 is a partial top plan view of the distal end of the polyp removal device of FIGS. 6 and 7, in a partially advanced position about a polyp;

FIG. 9 is a partial top plan view of the distal end of the polyp removal device of FIGS. 6-8, as the stalk of the polyp is being severed; and

FIG. 10 is a partial top plan view of another illustrative embodiment of a polyp removal device of the present disclosure, in a retracted position about a polyp.

DETAILED DESCRIPTION OF EMBODIMENTS

The foregoing summary, as well as the following detailed description will be better understood when read in conjunction with the appended figures. For the purpose of illustrating the present disclosure, various embodiments are shown. It is understood, however, that the present disclosure is not limited to the precise arrangement and instrumentalities shown.

As shown in the drawings and described throughout the following description, as is traditional when referring to relative positioning on an object, the term “proximal” refers to the end of the apparatus that is closer to the user and the term “distal” refers to the end of the apparatus that is further from the user.

Referring to FIGS. 1-4, an embodiment of the presently disclosed polyp removal device is shown therein and is generally designated as polyp removal device 100. Polyp removal device 100 includes an elongated tubular member 110, a handle portion 120 extending proximally from tubular member 110, and a snare portion or assembly 130 operably engaged with handle portion 120 and extending distally from within elongated tube 110. Polyp removal device 100 may be any suitable length and size for accessing various locations throughout the body. Device 100 may be configured for removal of suitable types of polyps of any size, or may be configured for general mucosal resection or removal of any suitable tissue mass. Preferably, polyp removal device 100 is configured for endoscopic, laparoscopic or transluminal insertion.

Referring initially to FIGS. 1-3, elongated tubular member 110 includes proximal and distal ends 110 a, 110 b. Proximal end 110 a of tubular member 110 is operably coupled to handle portion 120. As will be described in further detail below, handle portion 120 may be integrally formed with tubular member 110. Alternatively, handle portion 120 may be releasably secured to tubular member 110, or may instead be securely affixed to tubular member 110. Tubular member 110 may be flexible, semi-rigid, or rigid and may be constructed of metal, alloy, plastic, polymers, or any other suitable material. Distal end 110 b of tubular member 110 is configured to slidingly receive a proximal end of snare portion 130.

Although the following description of the polyp removal device 100 will be described in the form of a snare-type device, the aspects of the present disclosure may be modified for used with alternative handle configurations, including a pistol grip style device, mechanically and/or remotely actuated handles, other suitable types of devices or handle arrangements. As one example, polyp removal device 100 may be incorporated as a pistol grip style laparoscopic device like some of the LigaSure.™. tissue fusion devices sold by Valleylab of Boulder, Colo.

Still referring to FIGS. 1-3, handle portion 120 of polyp removal device 100 includes a base 122 coupled to proximal end 110 a of tubular member 110, a connector shaft 124 extending through base 122, and a handle 126 operably coupled to a proximal end 124 a of connector shaft 124. In one embodiment, base 122 of handle portion 120 may be securely affixed to proximal end 110 a of tubular member 110 using adhesive, bonding, mechanical fasteners, welding or other suitable methods. Alternatively, base 122 may be releasably connected to tubular member 110 using mechanical fasteners, threaded engagement, friction fitting, bayonet connections, or the like. In this manner, snare portion 130 may be removed and replaced through proximal end 110 a of tubular member 110. Base 122 of handle portion 120 may instead be integrally formed with proximal end 110 a of tubular member 110. Handle 126 is configured for operable engagement by a user. Handle 126 may be knurled or may include a coating for facilitating engagement by a user.

Base 122 of handle portion 120 is further configured for operable engagement with a generator 10. Base 122 defines a connection port 122 a for receiving an electrical cord 10 a extending from generator 10. Electrical cord 10 a extends from connection port 122 a through base 122 and is operably coupled to first and second electrodes 134, 136 of snare portion 130. Electrical cord 10 a may be directly coupled to first and second electrodes 134, 136. Alternatively, electrical cord 10 a may couple with a coupling member 123 mounted to shaft 124. In this manner, coupling member 123 electrically couples generator 10 with first and second electrodes 134, 136 along shaft 124. Generator 10 may include any suitable generator configured to selectively provide energy to electrodes 134, 136. For example, radiofrequency energy, either monopolar or bipolar may be provided to electrodes 134, 136. In other embodiments, ultrasonic, microwave, or laser energy may be provided. Depending on the energy modality utilized, snare 130 and/or electrodes 134, 136 may have to be reconfigured in order the handle the different types of energy.

In an embodiment where radiofrequency energy is utilized, to increase safety, bipolar radiofrequency energy is preferred because the energy will travel between first and second electrodes 134, 136 instead of between the snare 130 and some remote return pad. In one particular embodiment, generator 10 takes the form of a battery-powered generator that is integral with, or releasably coupled to, polyp removal device 100. In this example, electrical cord 10 a is not needed. Generator 10 may also be configured to monitor the electrical properties of the tissue maintained between first and second electrodes 134, 136 and signal to the clinician when conditions have been met that are suitable for sealing of tissue.

Still referring to FIGS. 1-3, connector shaft 124 includes an elongated tubular shaft including proximal and distal ends 124 a, 124 b. Proximal end 124 a is configured for operable engagement with handle 126. Handle 126 may be securely affixed, releasable coupled, or integrally formed with proximal end 124 a of connector shaft 124. Handle portion 120 may further include a stop member 128 positioned about connector shaft 124 between base 122 and handle 126. Stop member 128 prevents complete retraction of connector shaft 124 past base 122. Proximal end 124 a may be configured to securely retain stop member 128, or instead, may include grooves or indents 128 a for selectively positioning stop member 128 thereabout. In this manner, adjustment of stop member 128 reduces or increases the amount of extension of snare portion 130. Alternatively, stop member 128 may be configured to selectively engage distal end 124 a of connector shaft 124 through the incorporation of a mechanical fastener or the like (not shown). Distal end 124 b of connector shaft 124 is operably coupled to snare portion 130. Distal end 124 b may be permanently coupled, releasably coupled or integrally formed with snare portion 130.

Snare portion 130 includes a snare 132 formed of a loop of rigid or semi-rigid wire or flexible band. Snare 132 may be constructed of metal, polymer or other suitable material. In the illustrated embodiment, snare 132 is non-conductive; however, snare 132 may be conductive or partially conductive. Coupled to snare 132 in any suitable manner near a distal end 130 b of snare portion 130 are first and second electrodes 134, 136. As discussed above, first and second electrodes 134, 136 are electrically coupled to generator 10 to receive electrosurgical energy therefrom. First and second electrodes 134, 136, which may be of any suitable construction, each include at least a tissue contacting surface 134 c, 136 c. In some embodiments, first and second electrodes 134, 136 are each formed from a tissue contacting surface 134 c, 136 c and an insulative body portion. Tissue contacting surfaces 134 c, 136 c may include any configuration suitable for treating tissue, including hatching, grooves and detents (not shown). In one embodiment, generator 10, first and second electrodes 134, 136, and tissue contacting surfaces 134 c, 136 c, are all configured for sealing tissue.

Positioned between first and second electrodes 134, 136 is a connection member 133. Distal ends 134 b, 136 b of first and second electrodes 134, 136, respectively, are coupled to connection member 133. First and second electrodes 134, 136 and connection member 133 are configured such that in a first or extended position, proximal ends 134 a, 136 a of first and second electrodes 134, 136, respectively, are substantially spaced from one another. As will be discussed in further detail below, this configuration opens snare 132 to facilitate the looping of snare 132 over a polyp “P” (FIG. 6) and the positioning of first and second electrodes 134, 136 about stalk “S” of polyp “P”.

First and second electrodes 134, 136 and connection member 133 are further configured such that as proximal end 130 a of snare portion 130 is retracted within distal end 110 b of tubular member 110, proximal ends 134 a, 136 a of first and second electrodes 134, 136, respectively, are approximated towards each other, in the direction of arrows “A” (FIG. 1). In this manner, first and second electrodes 134, 136 and connection member 133 act like a jaw assembly, thereby compressing stalk “S” of polyp “P” between first and second electrodes 134, 136. To prevent first and second electrodes 134, 136 from contacting one another, distal end 110 b of tubular member 110 may include a spacer member 138 through which snare 132 may extend. Spacer member 138 spans distal end 110 b of tubular member 110 and includes a pair of apertures 138 a through which snare 132 is received. Apertures 138 a are spaced such that upon retraction of proximal end 130 a of snare portion 130 within tubular member 110, proximal end 134 a, 136 a of first and second electrodes 134, 136 are approximated towards one another. Apertures 138 a are further configured to prevent first and second electrodes 134, 136 contacting one another. Release of proximal end 130 a of snare portion 130 from within distal end 110 b of tubular member 100 permits proximal ends 134 a, 136 a of first and second electrodes 134, 136 to approximate away from one another and eventual return to their initial position.

In an alternative embodiment, one or both of first and second electrodes 134, 136 may include one or more spacers 134 d, 136 d (FIG. 5) formed on respective proximal ends 134 a, 136 a. Spacers 134 d, 136 d are configured to prevent contact between first and second electrodes 134, 136.

Connection member 133 extends between first and second electrodes 134, 136 and is configured to maintain distal ends 134 b, 136 b of first and second electrodes 134, 136, in a spaced relationship throughout the tissue excising procedure. As described above, in a first or extended position, proximal ends 134 a, 136 a of first and second electrodes 134, 136 are maintained in a substantially spaced apart relationship. This configuration facilitates positioning of snare 132, and first and second electrodes 134, 136 in particular, about stalk “S” of a polyp “P” (FIG. 6). Distal ends 134 b, 136 b of first and second electrodes 134, 136 are coupled to connection member 133 in a manner that permits pivoting, hinging, or flexing of first and second electrodes 134, 136 relative to connection member 133 as snare 132 is constricted about stalk “S” of polyp “P”. First and second electrodes 134, 136 and/or connection member 133 may be formed of flexible material, or may instead include a hinge mechanism or any other suitable configuration capable of permitting first and second electrodes 134, 136 to pivot, hinge, or flex relative to connection member 133. In the event that proximal ends 134 a, 136 a of first and second electrodes 134, 136 are approximated away from one another by the configuration of connection member 133, snare 132 may provide the spring force to maintain proximal ends 134 a, 136 a substantially spaced apart when polyp removal device 100 is in a first or extended position.

Connection member 133 further includes at least a first sharpened surface 133 a. First sharpened surface 133 a is formed between distal ends 134 b, 136 b of first and second electrodes 134, 136 and may be configured to severe stalk “S” of polyp “P” after proper sealing of the tissue. In addition, or alternatively, the outer surface of connection member 133 may be sharpened to facilitate excising of polyp “P”.

Referring now to FIGS. 1-3 and 6-8, one embodiment of the operation of polyp removal device 100 will be described. Initially, distal end 110 b of tubular member 110 is inserted into a patient. As discussed above, introduction of polyp removal device 100 may be accomplished through an endoscopic or laparoscopic port, or may be inserted transluminally through the mouth or anus. To facilitate insertion of tubular member 110 into the body, in one embodiment (FIG. 5), snare portion 130 a is completely retracted within tubular member 110.

Once distal end 110 b of tubular member 110 is positioned near a polyp “P” to be removed, snare portion 130 is extended distally by advancing handle 126 of handle portion 120 relative to base 122. The spring-like configuration between first and second electrodes 134, 136 and connection member 133 results in proximal ends 134 a, 136 a of first and second electrodes 134, 136 approximating away from each other as handle 126 is advanced and proximal end 130 a of snare portion 130 is released from tubular member 110. The separating of proximal ends 134 a, 136 a of first and second electrodes 134, 136 opens snare 132 and facilitates positioning of snare 132 about stalk “S” of polyp “P”. Once snare 132 positioned such that stalk “S” is received between first and second electrodes 134, 136, handle 126 may be retracted or, in the alternative, tubular member 110 may be advanced to constrict snare 132 about stalk “S”. As proximal end 130 a of snare portion 130 is received within distal end 110 b of tubular member 110 through spacer member 138, proximal ends 134 a, 136 a of first and second electrodes 134, 136 are approximated towards one another, thereby capturing stalk “S” of polyp “P” therebetween. Other methods of approximating first and second electrodes 134, 136 towards one another are contemplated by the present invention. For example, another instrument separate from polyp removal device 100 may be utilized.

Continued retraction of snare portion 130 within tubular member 110 causes first and second electrodes 134, 136 to compress stalk “S” of polyp “P”. Once the clinician is satisfied stalk “S” is sufficiently received between first and second electrodes 134, 136, generator 10 may be activated to treat the tissue between first and second electrodes 134, 136. Alternatively, and as discussed above, generator 10 may include a system for monitoring the electrical properties of the tissue between first and second electrodes 134, 136. Once a predetermined condition has been satisfied, preferably, a condition suitable to promote tissue sealing, generator 10 signals to the clinician that the tissue is ready to be sealed, at which point, generator 10 may automatically provide electrosurgical energy to tissue contacting surfaces 134 c, 136 c, or the clinician may activate generator 10 to provide the energy to seal the tissue. Electrosurgical energy is provided to tissue contacting surfaces 134 c, 136 c until the tissue of stalk “S” is properly sealed. Electrosurgical energy may be provided at a range of frequencies, over a variable duration, and may be continuous or intermittent, depending of the type of tissue being treated and the thickness of the tissue. Furthermore, the monitoring function may include for a signal to denote that the sealing is finished and that severing of the polyp “P” may take place.

In some embodiments, in order to effectively seal larger vessels (or tissue) two predominant mechanical parameters should be accurately controlled—the pressure applied to the vessel (tissue) and the gap distance between the electrodes—both of which are affected by the thickness of the sealed vessel. More particularly, accurate application of pressure may be important to oppose the walls of the vessel; to reduce the tissue impedance to a low enough value that allows enough electrosurgical energy through the tissue; to overcome the forces of expansion during tissue heating; and to contribute to the end tissue thickness, which is an indication of a good seal. It has been determined that a typical fused vessel wall is preferably between 0.001 and 0.006 inches. Below this range, the seal may shred or tear and above this range the lumens may not be properly or effectively sealed.

With respect to smaller vessels, the pressure applied to the tissue tends to become less relevant, whereas the gap distance between the electrically conductive surfaces becomes more significant for effective sealing. In other words, the chances of the two electrically conductive surfaces touching during activation increases as vessels become smaller.

As mentioned above, at least one electrode, e.g., 134, may include a stop member 134 d that limits the movement of the two opposing electrodes 134, 136 relative to one another. Stop member 134 d may extend from the tissue contacting surface 134 c a predetermined distance according to the specific material properties (e.g., compressive strength, thermal expansion, etc.) to yield a consistent and accurate gap distance “G” during sealing (FIG. 5). In one embodiment, the gap distance between opposing tissue contacting surfaces 134 c, 136 c during sealing ranges from about 0.001 inches to about 0.006 inches and, preferably, between about 0.002 and about 0.003 inches. The non-conductive stop members 134 d, 136 d may be molded onto electrodes 134, 136 (e.g., overmolding, injection molding, etc.), stamped onto electrodes 134, 136 or deposited (e.g., deposition) onto electrodes 134, 136. For example, one technique involves thermally spraying a ceramic material onto the surface of the electrodes 134, 136 to form the stop members 134 d, 136 d, respectively. Several thermal spraying techniques are contemplated that involve depositing a broad range of heat resistant and insulative materials on various surfaces to create stop members 134 d, 136 d for controlling the gap distance between electrically conductive surfaces 134 c, 136 c.

It has also been found that the pressure range for assuring a consistent and effective seal may be between about 3 kg/cm.sup.2 to about 16 kg/cm.sup.2 and, preferably, within a working range of 7 kg/cm.sup.2 to 13 kg/cm.sup.2. Manufacturing an instrument that is capable of providing a closure pressure within this working range has been shown, in some embodiments, to be effective for sealing arteries, tissues and other vascular bundles.

As can be appreciated, controlling the compressive force between with first and second electrodes 134, 136 as snare portion 130 is retracted may facilitate and assure consistent, uniform and accurate closure pressure about the tissue within the desired working pressure range of about 3 kg/cm.sup.2 to about 16 kg/cm.sup.2 and, preferably, about 7 kg/cm.sup.2 to about 13 kg/cm.sup.2. By controlling the intensity, frequency and duration of the electrosurgical energy applied to the tissue, the user can either cauterize, coagulate/desiccate, seal and/or simply reduce or slow bleeding.

In one embodiment, by controlling the force applied to handle 126, the resulting tension in snare portion 130 may be adjusted, which, in turn, regulates the overall pressure between electrodes 134, 136 to within the above-identified desired sealing range. A sensor 125 may be employed to accomplish this purpose and may be mechanically coupled to handle portion 120 and/or snare portion 130. A visual or audible indicator (not shown) may be operably coupled to handle portion 120, snare portion 130 and/or sensor 125 to provide visual, audible or tactile feed back to the user to assure that the clamping pressure is within the desired range prior to activation of the instrument.

Alternatively, handle portion 120 may incorporate a spring mechanism 125 a configured to prevent excessive force being applied to snare portion 130, thereby preventing overcompression of the tissue between first and second electrodes 134, 136. Spring mechanism 125 a may include a compression spring (not shown) that deforms once the force applied to handle 126 exceeds the force necessary to accomplish effective sealing between first and second electrodes 134, 136. In an alternative embodiment, snare portion 130 may instead be advanced and retracted through the rotation of handle 126. In this manner, handle portion 120 may include a torque mechanism, e.g., torque wrench or the like, (not shown) which is precisely set to measure the torque (rotational force) applied to snare portion 130 so the closure pressure between electrodes 134, 136 will fall within the desired pressure range.

Once the tissue of stalk “S” is sealed, handle 126 is partially advanced to extend a length of snare portion 130 from tubular member 110, thereby approximating proximal ends 134 a, 136 a of first and second electrodes, respectively, away from each other and exposing sealed stalk “S” to first sharpened surface 133 a of connection member 133. While maintaining snare portion 130 relative to tubular member 110, tubular member 110 is retracted relative to polyp “P”, thereby causing the engagement of stalk “S” with first sharpened surface 133 a of connection member 133. Continued retraction of tubular member 110 causes the complete severing of stalk “S” (see FIG. 9).

When using polyp removal device 110, the likelihood of excessive bleeding is greatly reduced because the tissue is completely sealed prior to being cut. Using polyp removal device 110 further reduces the likelihood of creating an open wound that is susceptible to infection. In addition, the utilization of bipolar energy to seal a polyp or other tissue is safer than monopolar, e.g., because of less thermal and energy spread, thereby reducing the likelihood of perforations.

With reference now to FIG. 10, an alternative embodiment of the present disclosure is shown generally as polyp removal device 200. Polyp removal device 200 is substantially similar to polyp removal device 100 and will, therefore, only be described as relates to the differences therebetween. Snare portion 230 includes first and second electrodes 234, 236 and a connection member 233. Extending between first and second electrodes 234, 236 and connection member 233 are extension members 235, 237, respectively. Extension member 235, 237 permit first and second electrodes 234, 236 to be spaced further apart from one another in a second or sealing condition. In this manner, polyp removal device 200 may be used to excise larger polyps having a larger stalk.

Various changes in form, detail and operation of the polyp removal devices of the present disclosure may be made without departing from the spirit and scope of the present disclosure. 

1. (canceled)
 2. A method of removing a tissue mass of a body, the method comprising: moving a snare portion of a tissue removal device relative to a spacer member of the tissue removal device; capturing the tissue mass with the snare portion; selectively delivering energy to the snare portion; and severing the tissue mass from the body with a sharpened surface of the snare portion.
 3. The method of claim 2, wherein selectively delivering energy to the snare portion further includes sealing the tissue mass.
 4. The method of claim 3, further comprising monitoring electrical properties of the tissue mass during energy delivery.
 5. The method of claim 4, further comprising detecting a predetermined condition of the tissue mass.
 6. The method of claim 5, further comprising signaling that the tissue mass is ready to be severed.
 7. The method of claim 2, further comprising preventing contact between a first portion of the snare portion and a second portion of the snare portion with the spacer member.
 8. The method of claim 2, further comprising retracting the snare portion relative to the tissue removal device to sever the tissue mass from the body.
 9. The method of claim 2, further comprising moving a handle of the tissue removal device relative to a tubular member of the tissue removal device to retract the snare portion.
 10. The method of claim 9, further comprising retracting at least a portion of the snare portion within the tubular member in response to axial movement of a connector shaft of the tissue removal device that is monolithically formed with ends of the snare portion.
 11. The method of claim 2, wherein selectively delivering energy to the snare portion includes selectively delivering energy from an electrosurgical generator operatively coupled to the tissue removal device.
 12. The method of claim 2, wherein moving the snare portion relative to the spacer member includes moving the snare portion through apertures defined in the spacer member. 